eve Conference Variant Block
Day 1 May 17, Thursday
8:30-9:00 Registration & Refresh Coffee
9:00-9:10 Welcome Remark
9:10-9:50 Mr. James J. HO, MD, PhD, DABCC,Professor, Director of Peking Union Medical College & Chinese Academy of Medical Sciences, Center for Clinical Laboratory Development; Chairman and CEO of Beijing Lawke Health Laboratory Co. Ltd.
Topic: Who Sets the Rules -- Chinese CRO Central Lab Going International
9:50-10:30 Mr. Charlie XU, MD, PhD, VP of Clinical Services at Frontage Lab China
Topic: Clinical CROs in China -- Prospective and Globalization
10:30-10:50 Coffee Break + Exhibition Visit
10:50-11:25 Mr. Zhenping WU, PhD, M.B.A. Senior Vice President, Pharmaceutical Sciences at HMP
Topic: Selection Criteria for Contract Organizations -- An Insider's View
11:25-12:00 Ms. Lin HE, PhD, Senior Director of Strategic Development Department of Shanghai Pharmaceutical Clinical Research Center
Topic: China and Global CRO Industrial Development Trends
12:00-13:30 Luncheon
13:30-14:10 Mr. Dan ZHANG, Chairman & CEO of Fountain Medical Development Ltd.
Topic: Managing Safety Issues in Clinical Development in China: The Role of CRO
14:10-14:50 Mr. Tony SONG, Manager of Life Science Market in 3M Purification division
Topic: Filtration Technologies in Pharmaceutical R&D Phase and 3M Validation Service
14:50-15:00 Q & A – All conference participants self-introduction
15:00-15:20 3M Release of Certification Laboratory
15:20-15:40 Coffee Break + Exhibition Visit
15:40-16:20 Ms. Weijun SHA, BD Director & Project Director of TigerMed
Topic: Creating New Valuable Working Model through Strategic Partnership with Clients
16:20-17:00 Panel Discussion – Q & A
Day2 May 18, Friday
9:00-9:40 Mr. Zhuohan HU, PhD, President & CEO, Research Institute for Liver Diseases (Shanghai) Inc.; Professor, Fudan University & Shanghai University of Chinese Medicines Shanghai, China
Topic: Bridging Discovery to Development in Therapeutic Innovation: Challenges and Solutions
9:40-10:20 Mr. James S. YAN, M.D. PhD, DABT, Senior Director and Site Scientific Lead of Covance Pharmaceutical R&D (Shanghai) Co., Ltd.
Topic: Project Management during Pharmaceutical Preclinical R&D: Study Design, Facilities and Data Interpretation
10:20-10:40 Coffee Break + Exhibition Visit
10:40-11:20 Mr. Yi YANG, PhD, RVT, Director of Preclinical Safety, DPE in Preclinical Safety of DSAR Asia-Pacific Sanofi-aventis China
Topic: Special Considerations in Preclinical Safety Assessment to Support Biopharmaceutical Development
11:20-12:00 Mr. Dylan Dalin YAO, MD, PhD, Senior VP & Chief Scientific Officer of Joinn Laboratories Inc.
Topic: Dual Solutions for Filing Nonclinical Pharm/Tox Data in Regulatory Submissions to Both the Domestic and International Agencies
12:00-13:30 Luncheon
13:30-14:10 Ms. Wen CAO, M.D, PhD, Manager of Phase I Clinical Trail in VPS Clinical Group.
Topic: Early Clinical Research on Drug Innovation
14:10-14:50 Mr. Ming GUO, PhD, Co-Founder & COO of Ascentage Pharma; General Manager of Small Molecule Drug R&D Center, China Medical City
Topic: An Experienced Partner in Late Discovery and IND Enabling at China Medical City
14:50-15:10 Coffee Break + Exhibition Visit
15:10-15:50 Mr. Zhenyu XUAN, PhD,General Manager of Suzhou Youseen New Drug R&D Co. Ltd., Senior Engineer; Professor of Shanghai University of TCM; Shanghai excellent academic leader
Topic: CRO Service for Traditional Chinese Medicine Development and the Entrance of TCM into Global Market
15:50-16:30 Panel Discussion – Q&A – Conference Conclusion
Package Plan
Before 29/2/2012: USD 440
After 29/2/2012: USD 540
eve Conference Detail Testimonial
Chinese companies and academics reaching out to the western scientific community through attending meetings, publishing in scientific journals, etc is very important to address this problem. By not publishing more it is not only hurting China's growth but global growth as the opportunity to collaborate on research and find out about new discoveries is limited.
——Seth Goldenberg, President of Asia Pacific Bio Intelligence LLC